The following data is part of a premarket notification filed by Elekta Instrument Ab with the FDA for Leksell Stereotactic System, Injection/ Aspiration Needle Kit.
| Device ID | K152558 |
| 510k Number | K152558 |
| Device Name: | Leksell Stereotactic System, Injection/ Aspiration Needle Kit |
| Classification | Neurological Stereotaxic Instrument |
| Applicant | ELEKTA INSTRUMENT AB KUNGSTENSGATAN 18, P.O. BOX 7593 Stockholm, SE Se-103 93 |
| Contact | Emma Widmark |
| Correspondent | Emma Widmark ELEKTA INSTRUMENT AB KUNGSTENSGATAN 18, P.O. BOX 7593 Stockholm, SE Se-103 93 |
| Product Code | HAW |
| CFR Regulation Number | 882.4560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-09-09 |
| Decision Date | 2016-03-02 |